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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216882Generated: October 25, 2026

Dimethylformamide → 2-(3-Cyanophenyl)-4-(pyridin-2-yl)-1,3-thiazole

https://huagongshe.com/reaction/2216882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-(3-Iodophenyl)-4-(pyridin-2-yl)-1,3-thiazoleHCID 10133344—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-(3-Cyanophenyl)-4-(pyridin-2-yl)-1,3-thiazoleHCID 996512130%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-(3-iodophenyl)-4-(pyridin-2-yl)-1,3-thiazole (1–30 mg, 0.36 mmol), zinc cyanide (117 mg, 1.0 mmol) and Pd(PPh3)4 (10 mg, 0.009 mmol) in N,N-dimethylformamide (2 mL) was heated overnight at 80° C. The mixture was cooled and diluted with toluene (5 mL). The organic solution was washed with 2N NH4OH (2×10 mL). The mixture was then extracted with ethyl acetate and the organic extract was washed with brine. The organic solution was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Silica gel chromatography afforded 28 mg (30%) of 2-(3-cyanophenyl)-4-(pyridin-2-yl)-1,3-thiazole: 1H-NMR (CDCl3), ppm: 8.65. (d, 1H), 8.38 (s, 1H), 8.25 (m, 2H), 8.15 (s, 1H), 7.85 (m, 1H), 7.72 (m, 1H), 7.6 (t, 1H), 7.28 (m, 1H). GC/EI-MS gave m/z 263 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112595B2
Source datasetuspto-grants-2006_09
ORD IDord-2c3c5e4c746b4b72988cd11efc9b6d03
Source noteuspto-grants-2006_09